ClinVar Miner

List of variants in gene INVS reported as likely benign by Preventiongenetics, part of Exact Sciences

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_014425.5(INVS):c.273+46C>T rs76975466 0.03524
NM_014425.5(INVS):c.740A>G (p.Asn247Ser) rs41312220 0.00526
NM_014425.5(INVS):c.3017-5T>G rs201018893 0.00177
NM_014425.5(INVS):c.2310C>T (p.His770=) rs116606949 0.00118
NM_014425.5(INVS):c.3153T>C (p.Tyr1051=) rs764214687 0.00003
NM_014425.5(INVS):c.1079-13G>C rs373264811 0.00002
NM_014425.5(INVS):c.1980A>G (p.Gly660=) rs139314036 0.00001
NM_014425.5(INVS):c.1131G>A (p.Leu377=) rs780406236
NM_014425.5(INVS):c.178A>C (p.Arg60=) rs886038603
NM_014425.5(INVS):c.2568G>A (p.Arg856=) rs886038604
NM_014425.5(INVS):c.615+13G>T rs761240492
NM_014425.5(INVS):c.849C>T (p.Ile283=) rs886038605

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